LQZClass II
Device, Jaw Repositioning
21 CFR 872.5570 / Dental
LQZ is the FDA product code for Device, Jaw Repositioning, a class II device type, regulated under 21 CFR 872.5570. As of , FDA records hold 27 510(k) clearances under this code, the most recent dated , and no recalls.
Classification record
- Product code
- LQZ
- Device name
- Device, Jaw Repositioning
- Regulation
- 21 CFR 872.5570
- Device class
- Class II
- Review panel
- Dental
- Submission type
- 510(k)
- Implant
- No
- Life sustaining or supporting
- No
- GMP exempt
- No
- Third party review eligible
- Yes
- Ingested clearances
- 27
- Ingested recalls
- 0
Clearances, product code LQZ
By decision yearShow the numbers
| Year | Clearances |
|---|---|
| 1987 | 1 |
| 1988 | 1 |
| 1990 | 1 |
| 1994 | 1 |
| 1995 | 4 |
| 1996 | 2 |
| 1997 | 1 |
| 2005 | 2 |
| 2006 | 2 |
| 2009 | 2 |
| 2011 | 1 |
| 2012 | 2 |
| 2013 | 1 |
| 2017 | 1 |
| 2020 | 2 |
| 2021 | 1 |
| 2023 | 1 |
| 2024 | 1 |
Applicants with the most clearances
Product code LQZ| Applicant | Clearances |
|---|---|
| Bryan Keropian Dds | 4 |
| Jonathan A. Parker, D.D.S. | 2 |
| Selane Products, Inc. | 2 |
| Achaemenid, LLC | 1 |
| Advanced Facialdontics, LLC | 1 |
| Aiomega, LLC | 1 |
| Biotex, Inc. | 1 |
| D.S.R.A., Inc. | 1 |
| Dental Crafters | 1 |
| Fellmar Company | 1 |
Companies listing this code with FDA
Companies whose registered establishments list this codeFIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.